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中国东北汉族人群中MTRR、TAF4B、PIWIL1基因变异与非梗阻性无精子症的关联研究

Association Study Between MTRR, TAF4B, PIWIL1 Variants and Non-Obstructive Azoospermia in Northeast Chinese Han Population.

作者信息

Yang Xiao, Zhang Hao, Jiang Yuting, Zhang Hongguo, Hu Xiaonan, Zhu Dongliang, Geng Dongfeng, Liu Ruizhi

出版信息

Clin Lab. 2018 Oct 1;64(10):1731-1738. doi: 10.7754/Clin.Lab.2018.180525.

Abstract

BACKGROUND

Non-obstructive azoospermia (NOA) is an important factor leading to male infertility and the genetic mechanism is not yet clear. It requires investigation to reveal its occurrence based on sequencing technology from the genetic level. Our previous genome wide association study (GWAS) using targeted high-throughput sequencing technology has identified suspected genetic variants including rs162036, rs161870, rs1677016R and rs1106042R associated with non-obstructive azoospermia (data not published).

METHODS

To further investigate the linkage between the four SNPs and the occurrence of NOA, 121 NOA patients and 256 controls were included. SNPs were detected by ligase detection reaction- polymerase chain reaction (LDRPCR). Association study between SNPs and NOA was analyzed.

RESULTS

As a result, we found no significant difference in all four alleles and genotypes frequencies in the SNPs between patients and controls (rs161870 p = 0.291; rs1677016R p = 0.264; rs161870 p = 0.291; rs1106042R p = 0.329).

CONCLUSIONS

The four SNPs are not shown to be significantly related with NOA. Therefore, the underlying potential genetic markers to Northeast Chinese Han population remain unclear and need to be further clarified.

摘要

背景

非梗阻性无精子症(NOA)是导致男性不育的重要因素,其遗传机制尚不清楚。需要基于测序技术从基因层面进行研究以揭示其发病原因。我们之前使用靶向高通量测序技术进行的全基因组关联研究(GWAS)已经确定了包括rs162036、rs161870、rs1677016R和rs1106042R在内的与非梗阻性无精子症相关的可疑基因变异(数据未发表)。

方法

为进一步研究这四个单核苷酸多态性(SNP)与NOA发病之间的联系,纳入了121例NOA患者和256例对照。通过连接酶检测反应-聚合酶链反应(LDRPCR)检测SNP。分析SNP与NOA之间的关联研究。

结果

结果发现,患者和对照之间SNP的所有四个等位基因和基因型频率均无显著差异(rs161870 p = 0.291;rs1677016R p = 0.264;rs161870 p = 0.291;rs1106042R p = 0.329)。

结论

这四个SNP未显示与NOA有显著相关性。因此,中国东北汉族人群潜在的遗传标记仍不清楚,需要进一步阐明。

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